Taiwan FDA registration 2276de0eb1a5aa3dc37cd8de0c773f7e
“Daeshin” NdYAG Laser System
TW: “黛欣”釹雅鉻雷射系統
Taiwan·Risk Class 2·MD·Daeshin Enterprise Co., Ltd.·Registered Jan 11, 2023 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- 2276de0eb1a5aa3dc37cd8de0c773f7e
- License Form
- Ministry of Health Medical Device Import No. 036272
- Customs Code
- DHA05603627208
Company information
- Manufacturer
- Daeshin Enterprise Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- ABIO MEDICAL SYSTEM COPR.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 11, 2023
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for “Daeshin” NdYAG Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2276de0eb1a5aa3dc37cd8de0c773f7e and manufactured by Daeshin Enterprise Co., Ltd.. The authorized representative in Taiwan is ABIO MEDICAL SYSTEM COPR..
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